пропозиції роботи
Wypowiedzi
-
[Author] Mariusz Olejniczak: [/ author]
>
Hi,I have a few questions for those involved in "medical writing". Or
>
I have a contact?@ Mariusz.olejniczak assigngroup.com
Hi Mariusz,
I have Freelance Medical Writters if you are interested please let me know.
Jack Korona -
I am looking for a Freelance Office Based Country Manager CRA Manager 0.5 FTE Eventually Becoming a Fulltime permanent staff with an up and coming international CRO for there Start up operations in Warsaw, Poland.
In this role we are looking for someone That is dynamic, has great business sense, hands on and very Operational.
You Must Travel Between 10% - 25% a month
You must have had previous clinical and line management experience, Especially in CRA mentoring, Conducting HR duties, Hiring CRA, ensuring That legal, fiscal, financial accounting and the welfare of the company in accordance with local law and Requirements group. Representing the company in and managing matters of local issues like legal, HR, administration, Training, Recruiting and Mentoring CRA's local line management, clinical staff and administrative staff, vendors and Interviewing candidates for positions CRA
Cv's to korona@hays.pl -
I am looking for a Freelance Office Based Country Manager/CRA Manager 0.5 FTE to eventually becoming Fulltime permanent staff with an up and coming international CRO for there Start up operations in Warsaw, Poland.
In this Role we are looking for someone that is Dynamic,has great business sense,hands on and very operational.
You must travel between 10%-%25 a month
You must have had previous clinical and line management experience, especially in CRA mentoring, Conducting HR duties, Hiring CRA, ensuring that legal, fiscal, financial and accounting welfare of the company in accordance with local law and group requirements. Representing the company in and managing matters of local issues like legal, HR, administration, Training, Recruiting and mentoring CRA’s Line management local clinical staff and administrative staff, Interviewing vendors and candidates for CRA positions
Cv’s to korona@hays.pl -
I am currently looking for Freelancer with more then 0.5FTE availability to start Mid May 2010
QA Auditor with proven record
Investigator Contract Associate
CRA with Maximum 3 years experience must have solid Oncology
CRA with Maximum 3 years experience must have solid CNS
CRA with Maximum 3 years experience must have solid Diabetes
CRA with Maximum 5 years experience must have solid Psychiatry,CNS
CTA with Minimum 5 years experience
Cv's to korona@hays.pl
Thank you
Jack Korona
Senior Consultant
Hays Pharma Poland
Also please visit my Freelance group on linkedin:
http://linkedin.com/groups?gid=2052923&trk=myg_ugr... -
I am currently looking for Freelancer with more then 0.5FTE availability to start Mid May 2010
QA Auditor with proven record
Investigator Contract Associate
CRA with Maximum 3 years experience must have solid Oncology
CRA with Maximum 3 years experience must have solid CNS
CRA with Maximum 3 years experience must have solid Diabetes
CRA with Maximum 5 years experience must have solid Psychiatry,CNS
CTA with Minimum 5 years experience
Cv's to korona@hays.pl
Thank you
Jack Korona
Senior Consultant
Hays Pharma Poland
Also please visit my Freelance group on linkedin:
http://linkedin.com/groups?gid=2052923&trk=myg_ugr... -
Role:
Working in partnership with a wide range of health professionals, organisations and patient groups, our client is always searching for new ways to promote and support these people and the work they do. Opportunities currently exist for a Primary Care Representative to join team covering territories across Poland promoting a product portfolio of leading market brands within the above product therapy areas. This role will have the possibility of some secondary care work depending on the territory business needs. With recent transformations to its field based business, Representatives now have the foundation to build stronger relationships with their customers and achieve greater autonomy and sales. Territory: Poland wide
Requirements:
Pharmaceutical sales experience preferred in area of Oncology or CN or Cardiology. You will have a successful sales track record you will be a good communicator, have excellent organisational skills and a sound knowledge of the Polish Health care system and Account Management. You will also have the ability to build and maintain strong customer relationships and positively affect patient care by influencing healthcare professionals on your territory. This is a unique opportunity to be a key player within an exciting venture and to share in its future success
Cv's to jacek.korona@hayspharma.com -
--Fix Term Contract 9 months-- Maternity Cover--Start July 2010
8000PLN to 10000PLN Monthly depending on experience
Our client is a global player in the field of health care. Its leading position is extended continuously by an innovative portfolio of medicines and the highly motivated and qualified team.
For the office in Warsaw we are looking for a competent, motivated:
Regulatory Affairs Specialist (m/f)
Principle Responsibilities
Provide regulatory guidance and support to RAST Team
Provide regulatory input to ensure acceptable labeling in no CEE/CIS markets
Establish/Maintain close working relationship between ERA and CEE/CIS colleagues
Ensure that regulatory management systems are employed to record day to day regulatory activities
Candidate Profile
A Good academic background with experience in Regulatory Affairs
Awareness of European Regulatory Procedures (MRP, DCP, CP) and regulatory procedures in non EU CEE/ CIS countries
Demonstrate excellent leadership and organizational skills to manage a multitude of countries and an effective liaison between European Regulatory Affairs and CEE Regulatory staff
Fluency in Polish and Good English preferably
Excellent negotiation and influencing skills
Capable to work in a matrix structure in a challenging environment
Positive work style, approachable, flexible and accountable
Attention to detail with analytical mind enabling assimilation of complex issues into a logical and presentable format
Balanced personality remaining calm under pressure and who is able to make decisions
Readiness to travel
IT literate and able to work with document management systems and databases
Please show your interest by contacting me on below email address
jacek.korona@hayspharma.com -
I am looking for 2 Senior Auditor's- Must have had experience in Audit's in Eastern Europe and have a proven track record.
You can either work 0.25FTE or 0.4FTE or 0.5FTE or 0.6FTE or 0.7FTE or above.
Strong English-Polish
Advantange if you speak some German or Italian or French or all but Ok if you dont.
Start date April 2010
Good Hourly rate
Aplicants can be based in most of Eastern Europe but preferably Poland
Please send Cv's to jacek.korona@hayspharma.com
or
Contact me directly on +44 207 922 7129
Jacek Korona
Senior Consultant Poland -
CONTRACT FREELANCE-Poland-HOME-BASED
- Submission Authorization Associate - 1FTE € 40 to € 45 per hour
depending on experience
Working within a highly qualified team you will prepare submissions
packages for the country specific Regulatory Authorities and Ethics
Committees for the region within which you work. You will liaise
with the authorities as appropriate regarding amendments and
questions Relating to start-up activities.
Additional Responsibilities:
Working proactively as part of a project team you will coordinate
all necessary activities required to gain Regulatory & Ethics
Committee approval for clinical studies.
You will be required to collate and prepare all documentation and
study regional dossiers for approval in accordance with the relevant
local legislations. In addition you will complete all amendments and
respond to queries related submission from the Clinical Teams.
Regular contact with the designated personnel from regulators
Authorities & Ethics Committees must be maintained in order to
Monitor progress of the submission in accordance with study start-up
deadlines.
Experience and Qualification
With a University degree in medicine, science, or equivalent, you
will have previous submissions / dossiers experience within clinical
studies for either a CRO or Pharma company. In addition you will
also require:
Knowledge of ICH GCP guidelines and expertise to review and evaluate
medical data
Demonstrate an understanding of regionally specific legislation
surrounding ethics committees and submissions procedures and
practices
Have excellent interpersonal and presentation skills and the ability
that interact at all levels in this client facing role
Bi-Lingual - you must be fluent native speaker with fluent Polish
since all submission documents to sponsors and many authorities must
be compiled in Polish
Ability to Prioritize work, have excellent attention to detail,
Demonstrate a pro-active attitude and have previously worked within
a team.
jacek.korona @ hayspharma.comJacek Korona edytował(a) ten post dnia 26.03.10 o godzinie 11:42
Dołącz do GoldenLine
Oferty pracy
Sprawdź aktualne oferty pracy
Aplikuj w łatwy sposób
Aplikuj jednym kliknięciem
